Kalaya Pain Relief Liquid
Product Images NDC 43493-0007

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Kalaya Pain Relief (NDC 43493-0007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avaria Health & Beauty Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Image Description (Updatedimage 1 V1)

Packaging label for Kalaya Pain Relief Spray Dry Touch, a topical pain relief liquid containing methyl salicylate, menthol, and camphor. The label shows a 2 fl oz (60 mL) bottle. Manufactured by Avaria Health & Beauty Corp in Canada. The front panel includes the brand name, product type, and dosage form, with drug facts and directions on side panels.*

FDA Label Image

Image Description (Updatedimage 2 V1)

The image shows the packaging label for Kalaya Pain Relief Spray, a topical liquid pain relief product containing menthol. The label features the Kalaya logo and branding, with hexagonal patterns in the background. It specifies that the spray is a dry touch formula and comes in a 2 fl oz (60 mL) bottle. The label includes drug facts, directions, warnings, manufacturer information (Avaria Health & Beauty Corp), and a barcode. Dimensions and layout markings for the carton are also visible.*

FDA Label Image

Image Description (Updatedimage 3 V1)

Kalaya Pain Relief Spray Dry Touch 2 fl oz (60 mL) topical liquid product label by Avaria Health & Beauty Corp. The label lists active ingredients as Camphor 10%, Menthol 8%, and Methyl Salicylate 25%, and highlights its use for temporary relief of minor muscle and joint pain. The product is made in Canada and includes Drug Facts and warnings including flammability and age restrictions.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.